Erythema multiforme-like cutaneous lesions in monomorphic epitheliotropic intestinal T-cell lymphoma: a rare case report

被引：12

作者：

Aiempanakit, Kumpol ^{[1
]}

Amatawet, Chitiarpa ^{[1
]}

Chiratikarnwong, Kanokphorn ^{[1
]}

Auepemkiate, Sauvarat ^{[2
]}

Kayasut, Kanita ^{[2
]}

Suwiwat, Supaporn ^{[2
]}

Apinantriyo, Benjawan ^{[3
]}

机构：

[1] Prince Songkla Univ, Div Dermatol, Dept Internal Med, Fac Med, Hat Yai 90110, Songkhla, Thailand

[2] Prince Songkla Univ, Dept Pathol, Fac Med, Hat Yai, Thailand

[3] Bangkok Hatyai Hosp, Hematol Unit, Songkhla, Thailand

来源：

JOURNAL OF CUTANEOUS PATHOLOGY | 2017年 / 44卷 / 02期

关键词：

enteropathy-associated T-cell lymphoma; erythema multiforme-like; monomorphic epitheliotropic intestinal T-cell lymphoma; pagetoid; ENTEROPATHY; CLASSIFICATION;

D O I：

10.1111/cup.12864

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL), also known as Type II enteropathy-associated T-cell lymphoma (EATL), is an aggressive peripheral T-cell lymphoma. EATL generally presents in adults with gastrointestinal symptoms. Skin involvement is very rare, found only in approximately five percent of patients. The authors report a 67-year-old Asian male who presented with chronic diarrhea and developed erythema multiforme-like cutaneous lesions. A skin biopsy revealed extensive pagetoid spread of atypical lymphocytes in the epidermis. The results of an immunohistochemistry test led to a diagnosis of MEITL. This report points to the need for dermatologists and dermatopathologists to consider a possible diagnosis of MEITL when encountering similar cases.

引用

页码：183 / 188

页数：6

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